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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579944Generated: October 30, 2026

2-Methylpyridine → 2-[3-(4-Phenoxyphenoxy)propyl]pyridine

https://huagongshe.com/reaction/579944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpyridineHCID 7975—
Reactant1-(2-Bromoethoxy)-4-phenoxybenzeneHCID 13254487—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-[3-(4-Phenoxyphenoxy)propyl]pyridineHCID 1415443952.4%

Reaction Conditions

Temperature-50 °C

Reaction Steps

To a solution of α-picoline (1.0 g, 11 mmol) in dry tetrahydrofuran (20 ml), n-butyl lithium (8 ml, 11 mmol; 1.4 mmol/ml) was added at -50° C. under nitrogen stream until the reaction mixture turned red. After stirring at -50° C. for 30 minutes, 2-(4-phenoxyphenoxy)ethyl bromide (3.0 g, 10 mmol) was dropwise added thereto at -50° C., and stirring was continued at the same temperature for 2 hours and at 20° C. for 12 hours. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was purified by silica gel column chromatography to give 2-[3-(4-phenoxyphenoxy)propyl]pyridine (1.6 g) as pale yellow oil. nD24.5 1.5861.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751225
Source datasetuspto-grants-1988_06
ORD IDord-cad3c7cf578348aa991e3141700c8d7c
Source noteuspto-grants-1988_06